FDA Label for Desonide
View Indications, Usage & Precautions
Desonide Product Label
The following document was submitted to the FDA by the labeler of this product Aleor Dermaceuticals Limited. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Package Label.Principal Display Panel
TUBE LABEL
Rx Only
NDC 71589-005-15
Desonide Ointment, 0.05%
FOR EXTERNAL USE ONLY
NOT FOR OPHTHALMIC USE
NET WT 15 grams
CARTON LABEL
Rx Only
NDC 71589-005-15
Desonide Ointment, 0.05%
FOR EXTERNAL USE ONLY
NOT FOR OPHTHALMIC USE
NET WT 15 grams
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